Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.
Genomic DNAs from twelve Japanese patients with steroid 21-hydroxylase [21-OHase; steroid 21-monooxygenase; steroid, hydrogen-donor:oxygen oxidoreductase (21-hydroxylating); EC 1.14.99.10] deficiency were analyzed by Southern blot hybridization. A 3.7-kilobase (kb) Taq I and a 1.7-kb Pvu II restrict...
Shranjeno v:
| izdano v: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
National Academy of Sciences
1987
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC299484/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3500473/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.84.22.8091 |
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